AU2006314309A1 - Process for the preparation of delmopinol and derivatives thereof - Google Patents

Abstract

A process for the preparation of delmopinol (3-(4-propylheptyl)-4-morpholinethanol) or a derivative or a pharmaceutically acceptable salt, or a solvate thereof, including a hydrate, comprises reacting oxazolidin [2,3-c]morpholine and a Grignard reagent, and optionally converting the delmopinol (or derivative) free base into a pharmaceutically acceptable salt. The oxazolidin [2,3-c]morpholine and the Grignard reagent are useful as intermediates in the production process.

Description

WO 2007/057681 PCT/GB2006/004293 PROCESS FOR THE PREPARATION OF DELMOPINOL AND DERIVATIVES THEREOF Field of the Invention The present invention relates to a process for the production of delmopinol or 5 a derivative thereof, as well as to intermediates useful in the production process. Background to the Invention Delmopinol is the International Non-proprietary Name (INN) of 3-(4-propylheptyl)-4-morpholinethanol (CAS No. 79874-76-3). Delmopinol hydrochloride salt (CAS No 98092-92-3) is intended to be used in the treatment of 10 gingivitis. The structure of delmopinol hydrochloride corresponds to formula: .HCI 15 OH Different processes for the production of delmopinol and its salts are known in the art. EP-A-038785 describes several processes to produce this compound. In particular, EP-A-038785 disclosed the preparation of delmopinol by alkylation of a 20 3-substituted morpholine, by dialkylation of a primary amine with a substituted bis(haloethyl)ether or a substituted diethyleneglycol disulfonate, by reduction of a diketomorpholine, or by transformation of the N-substituent of the morpholone into a hydroxyethyl group. EP-A-0426826 describes a process for the production of delmopinol which comprises a cycloaddition from a morpholine oxide to obtain a 25 morpholine-iso-oxazolidine, a reductive ring opening, followed by transformation of functional groups present in the side chain, and finally alkylation of the nitrogen to yield delmopinol. The known processes to produce delmopinol are long and require the use of some very toxic reagents, which make their industrial exploitation difficult and 30 expensive. Therefore, the provision of a new process for producing delmopinol is highly desirable. Summary of the Invention The current invention is based on the surprising realisation that delmopinol, and derivatives thereof, can be obtained by a short and convergent synthesis which takes WO 2007/057681 PCT/GB2006/004293 2 place through a reaction between an oxazolidin[2,3-c]morpholine compound and a Grignard compound. According to a first aspect of the present invention, a process for the production of a compound of formula (I) wherein R 1 is an alkyl or aryl moiety, or a 5 pharmaceutically acceptable salt, or a solvate thereof, including a hydrate, 0 OH N R1 10 L,, OH (I) 15 comprises reacting a compound of formula (II) with a grignard compound of formula (111) where X is an halogen selected from CI, Br and I and R 1 is an alkyl or aryl moiety, and optionally converting the compound of formula (I) free base obtained into a pharmaceutically acceptable salt. 20 2OO O XMg .O R1 25 (ll) (111) The inventors have also found an efficient production process of the new oxazolidin [2,3-c]morpholine (11), starting from commercially available diethanolamine which proceeds with high yields and purity. Therefore, a second aspect of the present 30 invention is the provision of a process for the production of oxazolidin[2,3-c]morpholine, which involves the reaction of diethanolamine with a (C 1

-C

4 )-alkyl haloacetate yielding the known 4-(2-hydroxyethyl)-morpholin-3-one, followed by a reduction reaction, to yield the oxazolidin[2,3-c]morpholine. Both steps can also be joined in a one pot reaction, avoiding the isolation of the 4-(2-hydroxyethyl)-morpholin-3-one. 35 WO 2007/057681 PCT/GB2006/004293 3 XMg (IliA) 5 According to a third aspect of the present invention, the production of a specific grignard compound (lilA) is carried out by treatment of a 1-halo-4-propylheptane with magnesium. According to a fourth aspect of the present invention is provided compounds 10 (II) and (IliA). These are useful as intermediates for the production of a compound of formula (IA). O 15 N OH (IA) According to a fifth aspect of the invention, compounds (11) and (111) are used 20 in the manufacture of a compound of formula (I). The process of the present invention is an easy and efficient alternative to manufacture delmopinol, derivatives of delmopinol and/or pharmaceutically acceptable salts thereof, on an industrial scale. The process is advantageous because it is a short and convergent synthesis, it avoids the use of toxic and flammable reagents, it 25 uses mild reaction conditions, and delmopinol is obtained with high yields and high purity. Detailed Description of the Invention A compound of formula (I) is produced according to the present invention. 0 30 R1 35 (I) OH WO 2007/057681 PCT/GB2006/004293 4 In the compound of formula (I), R, is an alkyl or aryl moiety. The alkyl or aryl moiety can be of any length, can be straight-chain or branched and can be substituted, i.e. can contain atoms other than carbon in the carbon backbone. As used herein, the terms "alkyl" and "aryl" are to be given their usual meanings on the art. Preferably, the alkyl 5 or aryl moiety comprises between 1 and 30 carbon atoms, more preferably between 2 and 20 carbon atoms, for example 6,7,8,9 or 10 carbon atoms. Compounds of formula (I) have been prepared where the R 1 group is a 1-Propyl, Benzyl, 1-Octyl, 1 Heptyl, 1-(2-ethyl)hexyl or 1-(2-propyl)hexyl group. The preparation of these compounds is described in Examples 6 to 11. 10 A preferred compound of formula (I) is delmopinol, which is represented below as formula (IA). In delmopinol, R 1 is a 4-propylheptyl chain. 15 N OH (IA) 20 According to the present invention, a compound of formula (I) is obtained by a reaction between the oxazolidin[2,3-c]morpholine (II) and the Grignard compound (Ill) where X is an halogen selected from CI, Br and I, and R, is an alkyl or aryl moiety as defined above and most preferably a 4-propylheptyl chain. A preferred compound of formula (111), wherein R, is a 4-propylheptyl chain is depicted as formula (lIliA) below. 25 XMg (lilA) 30 Most preferably, the compound of formula (111) is 4-propylheptylmagnesium bromide. As used herein, the term "Grignard Compound" is to be given its standard meaning, which is well known in the art, i.e. an organo-magnesium compound. For the avoidance of doubt, a compound of formula (I) is prepared by reacting 35 a compound of formula (11) with a Grignard compound of formula (III). A preferred WO 2007/057681 PCT/GB2006/004293 5 embodiment of this general reaction comprises the production of delmopinol (formula (IliA) by reacting a compound of formula (II) with the preferred Grignard compound of formula (lilA). The formation of the Grignard compound (Ill) and its subsequent reaction with 5 the oxazolidine (11) is carried out in a suitable solvent such as ethers (C 4

-C

1 2 ) and mixtures of said ethers with (C5-C) aliphatic or (C6-C8) aromatic hydrocarbons. Preferably the solvent is selected from the group consisting of diethylether, tetrahydrofuran, methyltetrahydrofuran, dibutylether and the following mixtures: tetrahydrofuran-toluene, tetrahydrofuran-xylene, methyltetrahydrofuran-toluene, 10 methyltetrahydrofuran-xylene, dibutylether-xylene, dibutylether-toluene. A compound of formula (I), for example delmopinol, obtained by the process of the present invention may be converted into a pharmaceutically acceptable salt, preferably into the hydrochloride salt, and delmopinol salts may be converted into delmopinol, by known methods described in the art. By a way of example, delmopinol 15 hydrochloride can be prepared from delmopinol by reaction with hydrochloric acid in any suitable solvent. Examples of suitable solvents are, for instance, toluene, xylene, methylisobutylketone, dibutylether, methyl-tert-butylether, ethyl acetate, and mixtures thereof. The compound of formula (11) can be obtained by the process summarised in 20 Scheme I, which can be carried out in two steps or as a one pot reaction. As used herein, the term "one pot reaction" is to be given its normal meaning in the art, i.e. the compound of formula (11) is produced in a single reaction vessel, such that at least a proportion of compounds (V) and (VI) are converted to compound (IV), and subsequently compound (II), without the isolation of intermediates. 25 The alternative to a one pot reaction is a two step reaction wherein formula (IV) is produced in a first step, and the second step of converting (IV) into (ll) is carried out separately. SCHEME I: 30 OH O Base NH + OR 1 N O N 0 OH I OH 35 (V) (VI) (IV) (ll) WO 2007/057681 PCT/GB2006/004293 6 In formula (VI), X is an halogen selected from Cl, Br and I, and R 1 is a

(C

1

-C

4 )-alkyl radical. Preferably the compound of formula (VI) is methyl chloroacetate. The reaction between the diethanolamine (V) and the haloacetate of formula (VI) is preferably carried out in the presence of a suitable base and a suitable solvent. 5 Examples of suitable bases are sodium hydride, sodium metoxide, potassium tert-butoxyde and sodium tert-butoxide. The best results are obtained with potassium tert-butoxide. Suitable solvents are for example tetrahydrofuran, xylene, toluene or dibutylether. The reaction between the diethanolamine (V) and the haloacetate (VI) can be 10 carried out at a temperature between room temperature and the reflux temperature of the solvent used. Preferably, the reaction is carried out at high temperatures (i.e. slightly less than the reflux temperature of the solvent, for example 50% of the reflux temperature or above, preferably 60%, 70%, 80% or 90% of the reflux temperature) to avoid thickness of the crude mixture by insolubility of diethanolamine alkoxyde at low 15 temperatures. Compound (IV) can be isolated from the reaction medium with high yield as an oil, which can be used without purification in the next step. If required, it can be purified by distillation. 3-Morpholinone (IV) can also be prepared by a process described in the literature (Australian Journal of Chemistry, 1996, vol. 49, pp. 1235-1242). However, this 20 process uses an excess of acylating reagent, it goes through an unstable intermediate and proceeds with low yields. The reduction of 3-morpholinone (IV) to yield the oxazolidine (11) is carried out using a reducing agent. Examples of reducing agents are sodium bis(2-methoxyethoxy)aluminum hydride (Vitride), sodium borohydride, lithium aluminiun 25 hydride and sodium bisethoxyaluminum hydride. A preferred reducing agent is sodium bis(2-methoxyethoxy)aluminum hydride. The reduction reaction is carried out in a solvent selected from a (C 6

-C

8 ) aromatic hydrocarbon such as toluene or xilene and an ether (C 4

-C

12 ) such as diethylether, tetrahydrofuran, dibutylether, methyl tert-butylether, and diethyleneglycol dibutyl ether. 30 Preferably, when the process of producing the compound of formula II is carried out in one pot, the alcohols generated during the reaction between the diethanolamine and the compound of formula (VI) are distilled before adding the reducing agent. The compound of formula (111) can be produced by reacting an alkyl or aryl halide with magnesium. Preferably, the halide is in the terminal or secondary position. 35 In a preferred embodiment, as illustrated in Scheme II, the compound of formula (lIliA) WO 2007/057681 PCT/GB2006/004293 7 is previously prepared by treating a compound of formula (VII) wherein X is an halogen selected from CI, Br, and I, with magnesium. Any suitable solvent for Grignard reactions such as ethers (C 4

-C

12 ) and mixtures of such ethers with (Cs-C,) aliphatic or

(C

6

-C

8 ) aromatic hydrocarbons can be used for the formation of Grignard compound. 5 The Grignard compound of formula (111) is not isolated and is used in solution. Its formation is easily detectable by the disappearance of magnesium and the brownish colouration of the solution. SCHEME II: 10 10 X + Mg - XMg (VII) (Il IA) 15 The compound of formula (VII) can be prepared from the corresponding hydroxy compound of formula (VIII) by an halogenation reaction. HO 20 (VIII1) Preferably in the compound of formula (VII), X is bromine and is preferably obtained by a brominating reaction of the compound (VIII) with aqueous hydrobromic 25 acid. The compound of formula (VIII) can be prepared by the process described in Justus Liebigs Annalen Chemie ,1966, vol. 693, p. 90, the content of which is hereby incorporated by reference. Throughout the description and claims the word "comprise" and variations of the word, such as "comprising", are not intended to exclude other technical features, 30 additives, components, or steps. Additional objects, advantages and features of the invention will become apparent to those skilled in the art upon examination of the description or may be learned by practice of the invention. The following examples are provided by way of illustration, and are not intended to be limiting of the present invention. 35 WO 2007/057681 PCT/GB2006/004293 8 EXAMPLES Example 1: Production of 4-(2-hydroxyethyl)morpholin-3-one (IV) 5 C N OH 10 Potassium tert-butoxyde (176 g, 1.1 eq.) was added to 1440 ml of toluene. The suspension was heated to 75 OC and maintained for 30 minutes until complete dissolution of the white solid. At this temperature diethanolamine (150 g, 1 eq.) was slowly added. The thick pale yellow suspension was maintained with strong stirring for 30 minutes and methyl chloroacetate (163 g, 1.05 eq.) was added slowly. The solution 15 was maintained at the same temperature for two hours. To the warm mixture methanol (600 ml) was added and cooled at room temperature, salts were filtrated and the organic layer concentrated until dry. Compound (IV) was obtained as an orange oil (204 g, 98%) which was distilled under high vacuum to obtain it as a highly pure colorless oil (80%, bp5 180 0 C). IR (film) (n cm-1): 3410, 2934, 2874,1633,1501,1350, 20 1141. MS (El), (m/z, %): 145 (M+., 12), 114 (M-CH2OH, 100), 86 (M-NC2H4OH, 65), 74 (M-71, 7), 56 (M-89, 41), 42 (M-103, 44). Example 2: Production of oxazolidin[2,3-clmorpholine (11) 25 0 30 To a solution of 3-morpholinone (IV) (207 g, 1 eq.) in toluene (1450 ml), Vitride solution (412 g, 2 eq., 70% in toluene) was slowly added at room temperature. The reaction was maintained for 15 min at this temperature. 50% aqueous sodium hydroxide solution (360 g, 3.15 eq.) was slowly added keeping the mixture at room temperature. The mixture was warmed to 50-60 OC and the aqueous layer was separated and 35 extracted at the same temperature with toluene (924 ml). Both organic layers were WO 2007/057681 PCT/GB2006/004293 9 concentrated together until dry. Oxazolidine (11) was obtained (154.5 g, 84%) as a brownish oil, which was distilled to give a highly pure colorless oil (65 g, bp2 80 OC). IR (film),(n cm-1): 2865, 1676, 1457,1297,1113,1046. MS (El), (m/z, %): 129 (M+., 50), 99 (M-CH20, 100), 98 (M-CH30, 90), 84 (M-C2H50, 10), 71 (M-C3H60, 51), 56 5 (M-73, 37), 42 (M-87, 47), 41 (M-88, 65). Example 3: Production of oxazolidin[2,3-c]morpholine (11) in a one-pot reaction starting from diethanolamine 10 Potassium tert-butoxyde (176 g, 1.1 eq.) was added to 1440 ml of toluene. The suspension was heated to 75 0 C and maintained for 30 min. until complete dissolution of the white solid. At this temperature diethanolamine (150 g, 1 eq.) was added slowly. The thick pale yellow suspension was maintained with strong stirring for 30 min. and methyl chloroacetate (163 g, 1.05 eq.) was added slowly. The solution was maintained 15 at the same temperature for two hours. Reaction mixture was cooled at 30 OC and Vitride solution (412 g, 2 eq., 70% in toluene) was added slowly at room temperature. The reaction was maintained for 30 min at this temperature. 50% aqueous sodium hydroxide solution (360 g, 3.15 eq.) was added slowly keeping the mixture at room temperature. The mixture was warmed to 50 OC and the aqueous layer was separated 20 and extracted at the same temperature with toluene (924 ml). Both organic layers were concentrated together until dry. Oxazolidine (11) was obtained (147 g, 80%) as a brownish oil. Example 4: Production of 4-(2-hydroxyethyl)-3-(4-propylheptyl)morpholine (IA) 25 OH 30 To a suspension of 1.3 g of magnesium (1 eq.) in 24 ml of toluene and 18 ml of tetrahydrofuran a small crystal of iodine was added. The mixture was heated at 64 0C and 12 g of 1-bromo-4-propylheptane (VII) (1 eq.) was added slowly controlling exothermicity of the reaction. The mixture was maintained at the same temperature for 35 2 hours and cooled at room temperature, obtaining a solution of compound (11l). A WO 2007/057681 PCT/GB2006/004293 10 solution of 7 g of oxazolidine (11) (1 eq.) in 7 ml of toluene was added to the previously prepared Grignard compound (I1) at room temperature in 30 min. 50 ml of toluene and 50 ml of saturated aqueous ammonium chloride solution were added and the resulting mixture was stirred at 40 0C until complete dissolution of salts, obtaining a biphasic 5 mixture. The organic layer was separated at 40 0C. The aqueous layer was extracted with 50 ml of toluene at 40 oC. Organic layers were concentrated together till dry, obtaining 8.8 g of 4-(2-hydroxyethyl)-3-(4-propylheptyl)morpholine as an orange oil. IR (film),(n cm-1): 3446, 2951,2925, 2859,1628,1458,1128,1048. MS (El), (m/z, %): 271 (M+., 1), 270 (M-H, 1), 240 (M-CH2OH, 46), 130 (M-141, 100), 100 (M-171, 29). 10 Example 5: Production of 4-(2-hydroxyethyl)-3-(4-propylheptyl) morpholine Hydrochloride 15 . HCI N OH To a solution of 7.4 g of crude 4-(2-hydroxyethyl)-3-(4-propylheptyl)morpholine in 22 20 ml of methyl iso-butyl ketone at room temperature concentrated hydrochloric acid (2.7g, 1 eq.) was added. The solution was concentrated until dry at 60 0C. The oil was dissolved again in 21 ml of methyl iso-butyl ketone the solution was seeded and stirred for 2 hours at 0 OC. The white solid was filtered, washed with 20 ml of cold methyl iso-butyl ketone and dried to obtain 5.9 g of 4-(2-hydroxyethyl)-3-(4-propylheptyl) 25 morpholine hydrochloride (delmopinol hydrochloride). 1H-NMR (CDC13, 400 MHz),( d ppm): 0.88 (6H, m, H15), 1.2-1.4 (13H, m), 1.8-2.0 (2H, m), 2.8-3.4 (5H, m), 3.4-4.4 (6H, m). 13C-NMR (CDCl3, 400 MHz),(d ppm): 14.26 (C15), 19.47,19.52 (C14), 22.87 (C10), 27.11 (C9), 33.25 (C11), 35.54,35.62 (C13), 36.59 (C12), 49.25 (C5), 53.20 (C7), 55.93 (C3), 57.08, 59.89 (C8), 63.1, 63.2, 65.0 (C6), 67.7 (C2). 30 Example 6: Synthesis of 4-(2-Hydroxyethyl)-3-propylmorpholine (IB) 1 6 0 ~ .. 2 47 OH 11 35 8 8 WO 2007/057681 PCT/GB2006/004293 11 43 g of Oxazolidine(ll) was dissolved in 215 ml of THF. At room temperature a solution of n-Propylmagnesiumchloride 20 % in THF (172 g, leq) was slowly added. The 5 mixture was stirred for 15 minutes. Mixture was concentrated until dryness under vacuum and 100 ml of Toluene and 64 g of saturated aqueous Ammonium Chloride solution were added and the resulting mixture was stirred at room temperature until complete dissolution of salts obtaining a biphasic mixture. Organic layerwas separated and aqueous layer was extracted with 265 ml of Toluene at room temperature. Organic 10 layers were concentrated together until dryness, obtaining 33.4 g of 4-(2-Hydroxyethyl)-3-propylmorpholine like a orange oil, which was further purified by column chromatography in silica gel eluting with a mixture of CH2CI2/MeOH/NH3 (99/1/1), obtaining the mentioned product as a colorless oil. 1H-NMR (CDCI3, 300 MHz),(d ppm): 0.92 (3H, t, J=7.2 Hz, H1 1), 1.36 (4H, m, H9/H10), 2.36 (3H, m, H3/H7), 15 2.82 (1H, ddd, J1=12.3, J2=4.9, J3=3.0 Hz, H5), 2.94 (1H, ddd, J1=12.3, J2=7.8, J3=4.8 Hz, H5), 3.44 (1H, dd, J1=11.2, J2=6.9 Hz, H2), 3.88 (1H, dd, J1=11.2, J2=4.9 Hz, H2), 3.62 (1H, dd, J1=4.8, J2=7.8 Hz, H6), 3.67 (1H, dd, J1=7.8, J2=4.9 Hz, H6), 3.75 (2H, m, H8). 13C-NMR (CDCI3, 75 MHz),(d ppm): 14.3 (C11), 19.3 (C10), 29.2 (C9), 49.9 (C5), 54.6 (C7), 57.7 (C8), 59.5 (C3), 66.9 (C6), 70.4 (C2). IR (film),(n 20 cm-1): 3444, 2958, 2863, 1456, 1366, 1129, 1052. MS (El), (m/z, %): 173 (M+., 42), 142 (M-CH2OH, 100), 130 (M-C3H7, 100), 112 (M-C3H7-H20, 14), 100 (M-73, 48), 84 (10), 71 (5), 56 (20), 42 (14). Example 7 of 4-(2-Hydroxyethyl)-3-(1-heptyl)morpholine(IC) 25 OH 30 200 g of 1-Bromoheptane were slowly added at 65 0 C to a suspension of 32.6 g of magnesium, 0.5 g of iodine and 2.4 ml of Dibromoetane in a mixture of 182 ml of THF and 400 ml of toluene. The reaction mixture was stirred at the same temperature for 3 h. When the formation of the corresponding Grignard compound was completed, the mixture was cooled down at room temperature and a solution of 158 g of Oxazolidine 35 (11) in 500 ml of toluene was added in 1 hour. The mixture was stirred for 30 min. and WO 2007/057681 PCT/GB2006/004293 12 then added to 795 ml solution of aqueous 5% HCi. The organic layer is decanted and concentrated until dryness. Compound (IC) was obtained as an orange oil (179 g). MS (El), (mlz, %): 229 (M+., 1), 198 (M-CH2OH, 25), 130 (M-C7H15, 100), 112 (M-C7H15-H20, 4), 100 (M-73, 30), 86 (5 56 (10), 41 (8). 5 Example 8: Synthesis of 4-(2-Hydroxyethyl)-3-benzylmorpholine(ID) 10 QOH Following the same procedure described for (IC) and starting from 10 g of Benzyl chloride and 11 g of Oxazolidine (11), 7.9 g of compound (ID) was obtained as an light yellow oil. MS (El), (m/z, %): 221 (M+., 1), 190 (M-CH2OH, 5), 130 (M-C7H7, 100), 91 15 (CH2C6H5, 8) Example 9: Synthesis of 4-(2-Hydroxyethyl)-3-(1-octyl)morpholine(IE) 20 K'OH 25 g of 1-Bromooctane were slowly added to a suspension of 3.5 g of magnesium and 7.5 mg of iodine in 41 ml of THF at 65 0 C. The reaction mixture was stirred at the same 25 temperature for 2 h. When the corresponding Grignard compound was prepared, the mixture was cooled down at 5 0 C and a solution of 16.7 g of Oxazolidine (11) in 40 ml of toluene was added in 1 hour. The mixture was stirred at 5 0 C for 30 min. and the reaction was warmed up until room temperature. The mixture was added to an aqueous solution of 5% HCI and stirred for 30 min. The organic layer was decanted, 30 dried and concentrated until dryness to obtain 19 g of the desired compound as a brown oil. MS (El), (m/z, %): 243 (M+., 5), 242 (M-H, 5), 212 (M-CH2OH, 50), 198 (M (CH2)20H, 8), 130 (M-C8H17, 100), 112 (M-C8H17-H20, 8), 100 (M-73, 30), 86 (8), 71 (8), 56 (9), 41 (14). 35 WO 2007/057681 PCT/GB2006/004293 13 Example 10: Synthesis of 4-(2-Hydroxyethyl)-3-(1-(2-ethylhexyl))morpholine(IF) 5 IOH Following the same procedure described for (IE) and starting from 25.5 g g of 1-Bromo-2-ethylhexane bromide and 16.2 g of Oxazolidine (11), 19.8 g compound (IF) were obtained as an dark orange oil. MS (El), (m/z, %): 243 (M+., 1), 214 (M-C2H5, 10 6), 212 (M-CH2OH, 11), 186 (M-C4H9, 4), 156 (8), 130 (M-C8H17, 100), 100 (46). Example 11: Synthesis of 4-(2-Hydroxyethyl)-3-(1-(2-propylpentyl))morpholine(lG) 15 N K IOH Following the same procedure described for (IE) and starting from 5.8 g g of 1-Bromo-2-propylpentane and 4 g of Oxazolidine (11), 3.3 g of compound (IF) were 20 obtained as an dark yellow oil. MS.(El), (m/z, %): 243 (M+., 1), 212 (M-CH2OH, 8), 200 (M-C3H7, 6), 170 (10), 130 (M-C8H17, 100), 100 (50).

Claims (18)

1. A process for the production of a compound of formula (I) wherein R, is an alkyl or aryl moiety, or a pharmaceutically acceptable salt, or a solvate thereof, 5 including an hydrate, O 10 N R1 OH (i) 15 which comprises reacting a compound of formula (11) with a Grignard compound of formula (111) wherein X is an halogen selected from CI, Br and I and R 1 is an alkyl or aryl moiety; and optionally converting the compound of formula (I) free base obtained into a pharmaceutically acceptable salt. 20 XMg N 0R N.O R4 (II) (Ill) 25

2. The process according to claim 1, wherein in formula (111) X is bromine.

3. The process according to claim 1 or claim 2, wherein formula (111) is formula (lilA) 30 (lilA) XMg 35 WO 2007/057681 PCT/GB2006/004293 15

4. The process according to claim 3, wherein the compound of formula (I) that is produced is formula (IA). OH 5 N O H (IA) 10

5. The process according to any preceding claim, wherein the reaction is carried out in a solvent selected from the group consisting of: ethers (C 4 -C 12 ) and mixtures of such ethers with (C 5 -C 8 ) aliphatic or (C 6 -C,) aromatic hydrocarbons, or combinations thereof. 15

6. The process according to any preceding claim, wherein the compound of formula (11) is obtained by a reduction reaction of a compound of formula (IV). 20 N (IV) OH 25

7. The process according to claim 6, wherein the reduction reaction is carried out with a reducing agent selected from sodium bis(2-methoxyethoxy)aluminum hydride, sodium borohydride, lithium aluminiun hydride, and sodium bisethoxyaluminum hydride.

8. The process according to claim 7, wherein the reducing agent is sodium 30 bis(2-methoxyethoxy)aluminum hydride.

9. The process according to any of the claims 6-8, wherein the reduction reaction is carried out in a solvent selected from a (C 6 -C 8 ) aromatic hydrocarbon and an ether (C 4 -C1 2 ). 35 WO 2007/057681 PCT/GB2006/004293 16

10. The process according to any of the claims 6-9, wherein the compound of formula (IV) is obtained by reaction of diethanolamine of formula (V) with a compound of formula (VI) wherein X is an halogen selected from CI, Br and I, and R1 is a 5 (C1-C4)-alkyl radical, in the presence of a base. OH OHO NH X 1-1OR 1 10 OH (V) (VI)

11. The process according to claim 10, wherein the base is selected from sodium hydride, sodium metoxide, potassium tert-butoxide and sodium tert-butoxide. 15

12. The process according to any of the claims 10-11, wherein the compound of formula (VI) is methyl chloroacetate.

13. The process of producing a compound of formula (ll) according to any of the 20 claims 6-12, which is carried out in a single reaction vessel.

14. The process according to any of the claims 3-13, wherein the Grignard compound of formula (IliA) is previously prepared by reacting a compound of formula (VII) wherein X is an halogen selected from the group consisting of Cl, Br and I, with 25 magnesium. x (VIl) 30 35 WO 2007/057681 PCT/GB2006/004293 17

15. A compound of formula (ll). N0 5 (ll)

16. A compound of formula (lilA), wherein X is an halogen selected from CI, Br, and 10 I. XMg 15 (lilA)

17. The compound according to claim 16, wherein X is bromine.

18. Use of a compound according to any of claims 15 to 17, in the manufacture of 20 delmopinol.